JPS62180366A

JPS62180366A - ハロゲン化銀写真感光材料

ハロゲン化銀写真感光材料

Info

Publication number: JPS62180366A
Authority: JP; Japan
Prior art keywords: group; groups; general formula; alkyl; silver halide
Prior art date: 1986-02-04
Legal status : Granted

Application number

JP2225986A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0562973B2 (enrdf_load_stackoverflow

Inventor

Shiyun Takada

高田　▲しゅん▼

Kaoru Onodera

薫小野寺

Current Assignee

Konica Minolta Inc

Original Assignee

Konica Minolta Inc

Priority date

1986-02-04

Filing date

1986-02-04

Publication date

1987-08-07

1986-02-04 Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc

1986-02-04 Priority to JP2225986A priority Critical patent/JPS62180366A/ja

1987-08-07 Publication of JPS62180366A publication Critical patent/JPS62180366A/ja

1993-09-09 Publication of JPH0562973B2 publication Critical patent/JPH0562973B2/ja

Status Granted legal-status Critical Current

Links

-1 Silver halide Chemical class 0.000 title claims abstract description 379
229910052709 silver Inorganic materials 0.000 title claims abstract description 101
239000004332 silver Substances 0.000 title claims abstract description 101
239000000463 material Substances 0.000 title claims abstract description 63
125000000217 alkyl group Chemical group 0.000 claims abstract description 174
125000001424 substituent group Chemical group 0.000 claims abstract description 138
150000001875 compounds Chemical class 0.000 claims abstract description 125
125000000623 heterocyclic group Chemical group 0.000 claims abstract description 74
239000000839 emulsion Substances 0.000 claims abstract description 58
239000003795 chemical substances by application Substances 0.000 claims abstract description 20
238000006243 chemical reaction Methods 0.000 claims abstract description 12
125000003118 aryl group Chemical group 0.000 claims description 114
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 90
125000003545 alkoxy group Chemical group 0.000 claims description 61
125000003342 alkenyl group Chemical group 0.000 claims description 60
125000000753 cycloalkyl group Chemical group 0.000 claims description 50
125000005843 halogen group Chemical group 0.000 claims description 49
125000002252 acyl group Chemical group 0.000 claims description 32
125000004104 aryloxy group Chemical group 0.000 claims description 29
238000009835 boiling Methods 0.000 claims description 23
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 22
125000005161 aryl oxy carbonyl group Chemical group 0.000 claims description 22
125000004093 cyano group Chemical group *C#N 0.000 claims description 17
239000000126 substance Substances 0.000 claims description 17
125000004414 alkyl thio group Chemical group 0.000 claims description 12
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 12
239000003960 organic solvent Substances 0.000 claims description 11
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 10
125000004422 alkyl sulphonamide group Chemical group 0.000 claims description 9
125000005110 aryl thio group Chemical group 0.000 claims description 9
125000004421 aryl sulphonamide group Chemical group 0.000 claims description 8
125000000962 organic group Chemical group 0.000 claims description 8
125000004391 aryl sulfonyl group Chemical group 0.000 claims description 7
125000005153 alkyl sulfamoyl group Chemical group 0.000 claims description 6
125000005115 alkyl carbamoyl group Chemical group 0.000 claims description 4
125000005116 aryl carbamoyl group Chemical group 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 abstract description 4
150000002367 halogens Chemical class 0.000 abstract description 4
239000010410 layer Substances 0.000 description 79
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 57
125000002887 hydroxy group Chemical group [H]O* 0.000 description 49
238000000034 method Methods 0.000 description 42
125000004429 atom Chemical group 0.000 description 32
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 32
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 32
MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 32
239000000975 dye Substances 0.000 description 31
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 28
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 26
125000004432 carbon atom Chemical group C* 0.000 description 25
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 22
150000003839 salts Chemical class 0.000 description 22
239000002245 particle Substances 0.000 description 18
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 17
239000000243 solution Substances 0.000 description 17
125000001624 naphthyl group Chemical group 0.000 description 16
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
150000002430 hydrocarbons Chemical group 0.000 description 15
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 15
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 15
125000000565 sulfonamide group Chemical group 0.000 description 15
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 15
108010010803 Gelatin Proteins 0.000 description 14
229910052801 chlorine Inorganic materials 0.000 description 14
229920000159 gelatin Polymers 0.000 description 14
239000008273 gelatin Substances 0.000 description 14
235000019322 gelatine Nutrition 0.000 description 14
235000011852 gelatine desserts Nutrition 0.000 description 14
150000003457 sulfones Chemical class 0.000 description 14
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
125000004423 acyloxy group Chemical group 0.000 description 13
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 13
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 13
238000010521 absorption reaction Methods 0.000 description 12
239000002253 acid Substances 0.000 description 12
229910052799 carbon Inorganic materials 0.000 description 12
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 12
239000000084 colloidal system Substances 0.000 description 12
239000013078 crystal Substances 0.000 description 12
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 12
229910052731 fluorine Inorganic materials 0.000 description 12
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 12
239000002904 solvent Substances 0.000 description 12
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 11
125000003277 amino group Chemical group 0.000 description 11
230000015572 biosynthetic process Effects 0.000 description 11
239000000460 chlorine Substances 0.000 description 11
230000000052 comparative effect Effects 0.000 description 11
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 10
125000003302 alkenyloxy group Chemical group 0.000 description 10
235000013339 cereals Nutrition 0.000 description 10
238000011161 development Methods 0.000 description 10
239000011737 fluorine Substances 0.000 description 10
229910052757 nitrogen Inorganic materials 0.000 description 10
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 10
238000003786 synthesis reaction Methods 0.000 description 10
238000012360 testing method Methods 0.000 description 10
238000011282 treatment Methods 0.000 description 10
HBEDSQVIWPRPAY-UHFFFAOYSA-N 2,3-dihydrobenzofuran Chemical compound C1=CC=C2OCCC2=C1 HBEDSQVIWPRPAY-UHFFFAOYSA-N 0.000 description 9
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 9
125000004442 acylamino group Chemical group 0.000 description 9
125000001931 aliphatic group Chemical group 0.000 description 9
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 9
229910052794 bromium Inorganic materials 0.000 description 9
239000006185 dispersion Substances 0.000 description 9
125000005842 heteroatom Chemical group 0.000 description 9
239000007788 liquid Substances 0.000 description 9
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 9
239000000203 mixture Substances 0.000 description 9
125000004433 nitrogen atom Chemical group N* 0.000 description 9
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 8
125000003368 amide group Chemical group 0.000 description 8
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 8
125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 8
KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 7
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 7
150000001721 carbon Chemical group 0.000 description 7
VZWXIQHBIQLMPN-UHFFFAOYSA-N chromane Chemical compound C1=CC=C2CCCOC2=C1 VZWXIQHBIQLMPN-UHFFFAOYSA-N 0.000 description 7
230000000694 effects Effects 0.000 description 7
230000008569 process Effects 0.000 description 7
238000012545 processing Methods 0.000 description 7
125000003003 spiro group Chemical group 0.000 description 7
229910052717 sulfur Inorganic materials 0.000 description 7
125000004417 unsaturated alkyl group Chemical group 0.000 description 7
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 6
206010070834 Sensitisation Diseases 0.000 description 6
125000002947 alkylene group Chemical group 0.000 description 6
125000000304 alkynyl group Chemical group 0.000 description 6
125000006038 hexenyl group Chemical group 0.000 description 6
229910000027 potassium carbonate Inorganic materials 0.000 description 6
235000011181 potassium carbonates Nutrition 0.000 description 6
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical compound N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 6
229920006395 saturated elastomer Polymers 0.000 description 6
230000008313 sensitization Effects 0.000 description 6
230000003595 spectral effect Effects 0.000 description 6
239000003381 stabilizer Substances 0.000 description 6
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 6
125000004149 thio group Chemical group *S* 0.000 description 6
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 5
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 5
239000002585 base Substances 0.000 description 5
239000007844 bleaching agent Substances 0.000 description 5
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 5
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 5
238000004040 coloring Methods 0.000 description 5
125000000392 cycloalkenyl group Chemical group 0.000 description 5
GLUUGHFHXGJENI-UHFFFAOYSA-N diethylenediamine Natural products C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 5
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
150000003413 spiro compounds Chemical group 0.000 description 5
238000006467 substitution reaction Methods 0.000 description 5
125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 5
239000011593 sulfur Substances 0.000 description 5
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
229960000583 acetic acid Drugs 0.000 description 4
229910052783 alkali metal Inorganic materials 0.000 description 4
229910000272 alkali metal oxide Inorganic materials 0.000 description 4
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 4
125000005129 aryl carbonyl group Chemical group 0.000 description 4
125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 4
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
238000004061 bleaching Methods 0.000 description 4
125000002837 carbocyclic group Chemical group 0.000 description 4
239000011248 coating agent Substances 0.000 description 4
238000000576 coating method Methods 0.000 description 4
239000003086 colorant Substances 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
239000001257 hydrogen Substances 0.000 description 4
230000002209 hydrophobic effect Effects 0.000 description 4
NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 4
HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical group CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 description 4
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
QWOKKHXWFDAJCZ-UHFFFAOYSA-N octane-1-sulfonamide Chemical group CCCCCCCCS(N)(=O)=O QWOKKHXWFDAJCZ-UHFFFAOYSA-N 0.000 description 4
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 4
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 4
125000005499 phosphonyl group Chemical group 0.000 description 4
239000000049 pigment Substances 0.000 description 4
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 4
230000001235 sensitizing effect Effects 0.000 description 4
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 4
238000003860 storage Methods 0.000 description 4
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
239000006097 ultraviolet radiation absorber Substances 0.000 description 4
239000000052 vinegar Substances 0.000 description 4
235000021419 vinegar Nutrition 0.000 description 4
229910052727 yttrium Inorganic materials 0.000 description 4
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 3
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
244000046052 Phaseolus vulgaris Species 0.000 description 3
239000004698 Polyethylene Substances 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 3
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 3
239000000654 additive Substances 0.000 description 3
125000004448 alkyl carbonyl group Chemical group 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
125000005162 aryl oxy carbonyl amino group Chemical group 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
125000004744 butyloxycarbonyl group Chemical group 0.000 description 3
239000001913 cellulose Substances 0.000 description 3
229920002678 cellulose Polymers 0.000 description 3
125000001309 chloro group Chemical group Cl* 0.000 description 3
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
DROMNWUQASBTFM-UHFFFAOYSA-N dinonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC DROMNWUQASBTFM-UHFFFAOYSA-N 0.000 description 3
238000001035 drying Methods 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 3
238000011156 evaluation Methods 0.000 description 3
238000005562 fading Methods 0.000 description 3
229930195733 hydrocarbon Natural products 0.000 description 3
125000002883 imidazolyl group Chemical group 0.000 description 3
125000005462 imide group Chemical group 0.000 description 3
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 3
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
125000002801 octanoyl group Chemical group C(CCCCCCC)(=O)* 0.000 description 3
125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 3
125000006678 phenoxycarbonyl group Chemical group 0.000 description 3
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 3
150000003014 phosphoric acid esters Chemical class 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
230000001681 protective effect Effects 0.000 description 3
239000011241 protective layer Substances 0.000 description 3
125000000714 pyrimidinyl group Chemical group 0.000 description 3
230000005070 ripening Effects 0.000 description 3
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
210000002784 stomach Anatomy 0.000 description 3
NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical group NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 3
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 3
229910052724 xenon Inorganic materials 0.000 description 3
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 3
125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 2
KOFZTCSTGIWCQG-UHFFFAOYSA-N 1-bromotetradecane Chemical compound CCCCCCCCCCCCCCBr KOFZTCSTGIWCQG-UHFFFAOYSA-N 0.000 description 2
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
JKRNNIGZNCVVHA-UHFFFAOYSA-N 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate;trimethylazanium Chemical compound C[NH+](C)C.C[NH+](C)C.C[NH+](C)C.C[NH+](C)C.[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O JKRNNIGZNCVVHA-UHFFFAOYSA-N 0.000 description 2
125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 2
ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 description 2
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